Sponsors & CROs

ACRC Trials

Today’s Research. Tomorrow’s Medicine.

At ACRC Trials, we understand the vital role Sponsors and CROs play in advancing medical innovation. Established in 2005, ACRC Trials has built a strong reputation as a premier clinical research investigator site network in Texas by earning the trust of pharmaceutical sponsors and contract research organizations (CROs). We consistently deliver high-quality data across Phase I, II, III, and IV outpatient clinical trials – including vaccine studies, across a wide range of therapeutic areas.

ACRC Trials is recognized for our rapid study start-up capabilities, strong patient enrollment performance, precise regulatory-compliant documentation, efficient SOP-driven trial execution, and unmatched dedication to quality assurance.

Our experienced team is known for being responsive, flexible, and collaborative. We offer a seamless experience from study feasibility and startup to closeout, ensuring each trial receives the attention it deserves.
Sponsors and CROs routinely commend us for our professionalism, site efficiency, and ability to meet and exceed enrollment targets and data delivery timelines. We consistently surpass expectations by providing accurate, complete clinical trial data on time and with the highest standards of compliance.


ACRC Trials has the expertise, infrastructure, and commitment to make your clinical research a success.

Quality is Our Priority

ACRC Trials is committed to delivering high-quality data and services to our sponsors by implementing protocols efficiently and ethically, thus enabling sponsors to accelerate the drug development process. Our team leads the way in leveraging cutting-edge digital technology throughout clinical trials, optimizing the entire process for greater efficiency and effectiveness.

Utilizing e-source, e-regulatory (eTMF), e-stipend, CTMS, and remote monitoring, we minimize errors and bolster accuracy. By embracing real-time, centralized data collection, we ensure efficient and precise data entry and analysis.

We take pride in our mission to provide exceptional services to our sponsors and volunteers, ensuring that patients can enjoy the benefits of approved treatments as quickly as possible. Our commitment to excellence, reliability, and volunteer care has earned us recognition, with more investigators recognized by their peers than any other research facility in Texas.

We welcome an invitation for dialogue regarding new research opportunities and look forward to cultivating long-term relationships with Sponsors and Clinical Research Organizations.

Why Partner with ACRC Trials?

  • Experienced Principal Investigators: Our team comprises dedicated physician investigators, nurse practitioners, and physician assistants who maintain close oversight of all studies, ensuring rigorous attention to detail and adherence to protocols.
  • Skilled Study Coordinators: Our research coordinators possess extensive medical training and solid backgrounds in research, supported by administrative staff, research assistants, a dedicated recruitment department, regulatory specialists, and contracts & budgets personnel.
  • State-of-the-Art Facilities: Our modern clinics are fully equipped to handle a wide array of clinical trials, providing a comfortable and safe environment for participants.
  • Patient-Centric Approach: We prioritize effective communication and accessibility, fostering positive relationships with both patients and Sponsors. Our commitment to patient care ensures high retention rates and reliable data.
  • Established in 2005: ACRC Trials has a proven reputation for producing high-quality data. We routinely receive recognition from Sponsors and CROs for our dedication to making each study a success, adhering to Standard Operating Procedures, and maintaining comprehensive and professional documentation.

Facility Description

  • 9 large practices in Texas
  • Total database of over 430,000 patients
  • Dedicated Research SUITES
  • Dedicated monitoring & conference rooms
  • Teams dedicated to vaccine trials
  • Experienced Clinical Research Coordinators
  • Dedicated Recruiters
  • Dedicated Regulatory Personnel
  • Contracts & Budgets Personnel
  • Clinical Trial Management Software
  • E-Source
  • E-Regulatory
  • Ethnically diverse population
  • Climate and access-controlled storage rooms
  • Extended hours to accommodate patients
  • Central IRB
  • Sophisticated and comprehensive SOPs
  • Excellent Source Documents

Therapeutic Areas

  • Asthma, Allergy & Immunology
  • Cardiology
  • Dermatology  (Adult & Pediatrics)
  • Ear, Nose & Throat (Otolaryngology)
  • Endocrinology, Diabetes & Metabolism
  • Family Medicine
  • Internal Medicine
  • Men’s Health
  • Neurology & Headache
  • Pediatrics
  • Vaccines  (Adult & Pediatrics)
  • Women’s Health

Our Locations

ACRC Trials is headquartered in West Plano and operates research sites across the Dallas–Fort Worth metroplex, including Frisco, Carrollton, and Grapevine, as well as in the greater Austin area.

Our locations are strategically positioned to serve a broad, ethnically diverse population, allowing us to conduct high-quality clinical trials that reflect real-world demographics. This diversity strengthens the relevance of our data and supports more inclusive, impactful research outcomes.

Contact Us

Partner with ACRC Trials to ensure your clinical research is conducted with excellence and integrity.

Reach out to us at (214) 379-ACRC (2272) or fill out the form below for a callback to discuss how we can collaborate on your next study.

Together, we can advance medical treatments and bring tomorrow’s medicine to today’s patients.
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